Present status of germline findings in precision medicine for Japanese cancer patients: issues in the current system

Author:

Higashigawa Satomi1,Matsubayashi Hiroyuki12ORCID,Kiyozumi Yoshimi1,Kado Nobuhiro13,Nishimura Seiichiro14,Oishi Takuma5,Sugino Takashi5,Fushiki Kunihiro6,Shirasu Hiromichi6,Yasui Hirofumi6,Mamesaya Nobuaki7,Fukuzaki Naomi8ORCID,Kunitomo Kana8,Horiuchi Yasue1910,Kenmotsu Hirotsugu17,Serizawa Masakuni1112

Affiliation:

1. Division of Genetic Medicine Promotion

2. Endoscopy

3. Gynecology

4. Breast Surgery

5. Pathology

6. Gastrointestinal Oncology

7. Thoracic Oncology

8. Nursing

9. Department of Psychiatry and Behavioral Sciences , , Setagaya-ku, Tokyo, Japan

10. Tokyo Metropolitan Institute of Medical Science , , Setagaya-ku, Tokyo, Japan

11. Clinical Research Center , , Nagaizumi-cho, Sunto-gun, Shizuoka, Japan

12. Shizuoka Cancer Center , , Nagaizumi-cho, Sunto-gun, Shizuoka, Japan

Abstract

Abstract Objective Since 2019, precision cancer medicine has been covered by national insurance in Japan; however, to date, germline findings have not been fully reported. The aim of this study was to evaluate the current status and raise a problem of germline finding analysis and disclosure in Japanese precision cancer medicine. Methods Germline findings of 52 genes were examined in 296 cases with advanced cancer by a case series study. Results Six (2.0%) cases were examined by the Oncoguide™ NCC Oncopanel with germline testing, but no germline findings were reported. The remaining 290 (98.0%) cases were analyzed by FoundationOne® CDx (tumor-only testing), which recognized 404 pathogenic variants; those of BRCA1/2 were recognized in 16 (5.5%) tumors. Our institutional algorithm suggested 39 candidate germline findings in 34 cases, while the public algorithm listed at least 91 candidate germline findings. Four germline findings had been previously identified (BRCA1: 3 and ATM: 1). Nine of 30 cases with candidate germline findings excluding these known germline findings refused or deferred germline testing. Only 4 of 16 cases that received counseling underwent germline testing, and those 4 revealed 3 germline findings (BRCA2, CDK4 and RAD51C); in total, 8 (2.7%) germline findings were revealed. Reasons for refusing genetic counseling and/or germline testing included extra hospital visits, added expense for germline testing due to limited national insurance coverage, poor patient physical condition and no known family members associated with the possible germline finding. Conclusions In current Japanese precision cancer medicine, only a small fraction of the patients undergoes germline testing and demonstrated germline finding. The current results suggested a need for earlier indications for precision cancer medicine, broader insurance coverage and more efficient germline finding prediction algorithms, to increase the number of germline testings and to improve the following managements.

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Radiology, Nuclear Medicine and imaging,Oncology,General Medicine

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